Page last updated: 2024-11-07

c 1310

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

C 1310: an imidazoacridinone; arrests cell-cycle progression in the G2 phase of L1210 cells; structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID132128
CHEMBL ID125082
SCHEMBL ID13526631
MeSH IDM0259897

Synonyms (17)

Synonym
3s0283z6w9 ,
138154-40-2
unii-3s0283z6w9
nsc-637992
NCI60_012641
c 1310
6h-imidazo(4,5,1-de)acridin-6-one, 5-((2-(diethylamino)ethyl)amino)-8-hydroxy-1-methyl-
ccris 7539
5-((2-(diethylamino)ethyl)amino)-8-hydroxy-1-methyl-6h-imidazo(4,5,1-de)acidin-6-one
CHEMBL125082 ,
5-(2-(diethylamino)ethylamino)-8-hydroxy-1-methyl-6h-imidazo[4,5,1-de]acridin-6-one
5-(2-diethylamino-ethylamino)-8-hydroxy-1-methyl-2,10b-diaza-aceanthrylen-6-one(1.5mhcl.0.5mh2o)
bdbm50008344
C-1310 ,
SCHEMBL13526631
DTXSID70160509
Q27257958
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Protein Targets (1)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Ribosyldihydronicotinamide dehydrogenase [quinone]Homo sapiens (human)IC50 (µMol)0.03500.00271.62879.9000AID479979; AID621612
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (1)

Processvia Protein(s)Taxonomy
quinone catabolic processRibosyldihydronicotinamide dehydrogenase [quinone]Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (12)

Processvia Protein(s)Taxonomy
dihydronicotinamide riboside quinone reductase activityRibosyldihydronicotinamide dehydrogenase [quinone]Homo sapiens (human)
protein bindingRibosyldihydronicotinamide dehydrogenase [quinone]Homo sapiens (human)
zinc ion bindingRibosyldihydronicotinamide dehydrogenase [quinone]Homo sapiens (human)
electron transfer activityRibosyldihydronicotinamide dehydrogenase [quinone]Homo sapiens (human)
oxidoreductase activityRibosyldihydronicotinamide dehydrogenase [quinone]Homo sapiens (human)
oxidoreductase activity, acting on other nitrogenous compounds as donorsRibosyldihydronicotinamide dehydrogenase [quinone]Homo sapiens (human)
chloride ion bindingRibosyldihydronicotinamide dehydrogenase [quinone]Homo sapiens (human)
protein homodimerization activityRibosyldihydronicotinamide dehydrogenase [quinone]Homo sapiens (human)
FAD bindingRibosyldihydronicotinamide dehydrogenase [quinone]Homo sapiens (human)
melatonin bindingRibosyldihydronicotinamide dehydrogenase [quinone]Homo sapiens (human)
resveratrol bindingRibosyldihydronicotinamide dehydrogenase [quinone]Homo sapiens (human)
NAD(P)H dehydrogenase (quinone) activityRibosyldihydronicotinamide dehydrogenase [quinone]Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (3)

Processvia Protein(s)Taxonomy
nucleoplasmRibosyldihydronicotinamide dehydrogenase [quinone]Homo sapiens (human)
cytosolRibosyldihydronicotinamide dehydrogenase [quinone]Homo sapiens (human)
extracellular exosomeRibosyldihydronicotinamide dehydrogenase [quinone]Homo sapiens (human)
cytosolRibosyldihydronicotinamide dehydrogenase [quinone]Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (12)

Assay IDTitleYearJournalArticle
AID479979Inhibition of human recombinant NQO2 assessed as reduction of DCPIP by spectrophotometry2010Bioorganic & medicinal chemistry letters, May-01, Volume: 20, Issue:9
Imidazoacridin-6-ones as novel inhibitors of the quinone oxidoreductase NQO2.
AID621613Cytotoxicity against human HCT116 cells after 24 hrs by MTT assay2011Journal of medicinal chemistry, Oct-13, Volume: 54, Issue:19
Novel inhibitors of NRH:quinone oxidoreductase 2 (NQO2): crystal structures, biochemical activity, and intracellular effects of imidazoacridin-6-ones.
AID621612Inhibition of human recombinant NQO2 assessed as reduction of DCPIP by spectrophotometry2011Journal of medicinal chemistry, Oct-13, Volume: 54, Issue:19
Novel inhibitors of NRH:quinone oxidoreductase 2 (NQO2): crystal structures, biochemical activity, and intracellular effects of imidazoacridin-6-ones.
AID621614Cytotoxicity against human HCT116 cells after 96 hrs by MTT assay2011Journal of medicinal chemistry, Oct-13, Volume: 54, Issue:19
Novel inhibitors of NRH:quinone oxidoreductase 2 (NQO2): crystal structures, biochemical activity, and intracellular effects of imidazoacridin-6-ones.
AID139781Antineoplastic activity was evaluated in vivo against murine leukemia P388 (i.p./i.p.; days 1-5) and optimum dose was reported1992Journal of medicinal chemistry, Jan-24, Volume: 35, Issue:2
Chromophore-modified antineoplastic imidazoacridinones. Synthesis and activity against murine leukemias.
AID100464In vitro inhibitory activity against murine L1210 leukemia1992Journal of medicinal chemistry, Jan-24, Volume: 35, Issue:2
Chromophore-modified antineoplastic imidazoacridinones. Synthesis and activity against murine leukemias.
AID136250In vivo % T/C activity was measured against P388 leukemia; 2901992Journal of medicinal chemistry, Jan-24, Volume: 35, Issue:2
Chromophore-modified antineoplastic imidazoacridinones. Synthesis and activity against murine leukemias.
AID134763Toxicity in CDF1 male mice following a single intraperitoneal administration1992Journal of medicinal chemistry, Jan-24, Volume: 35, Issue:2
Chromophore-modified antineoplastic imidazoacridinones. Synthesis and activity against murine leukemias.
AID479981Binding affinity to calf thymus DNA assessed as change in melting temperature at 10 uM relative to control2010Bioorganic & medicinal chemistry letters, May-01, Volume: 20, Issue:9
Imidazoacridin-6-ones as novel inhibitors of the quinone oxidoreductase NQO2.
AID1096392Binding affinity to Bos taurus (calf) thymus DNA assessed as change in melting temperature at drug to DNA base pair ratio 0.25 M2011Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents, Nov, Volume: 20, Issue:8
Physicochemical interaction of antitumor acridinone derivatives with DNA in view of QSAR studies.
AID1096393Antitumor activity against Mus musculus (mouse) P388 cells xenografted in Mus musculus (mouse) assessed as increase in survival time relative to control2011Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents, Nov, Volume: 20, Issue:8
Physicochemical interaction of antitumor acridinone derivatives with DNA in view of QSAR studies.
AID479980Toxicity in human HCT116 cells after 96 hrs by MTT assay2010Bioorganic & medicinal chemistry letters, May-01, Volume: 20, Issue:9
Imidazoacridin-6-ones as novel inhibitors of the quinone oxidoreductase NQO2.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (6)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's3 (50.00)18.2507
2000's0 (0.00)29.6817
2010's3 (50.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 47.30

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index47.30 (24.57)
Research Supply Index1.95 (2.92)
Research Growth Index4.64 (4.65)
Search Engine Demand Index66.20 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (47.30)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other6 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]